Potassium Chloride In Dextrose
NDC Package 0264-7628-00

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was discontinued by the firm.

Potassium Chloride In Dextrose is this intravenous solution is indicated for use in adults and pediatric patients as a source of electrolytes, calories, and water for hydration. Marketed by B. Braun Medical Inc., this product is identified by NDC 0264-7628 and is authorized under FDA application NDA019699.

Identification & Billing

NDC Package Code
0264-7628-00
Package Description
12 CONTAINER in 1 CASE / 1000 mL in 1 CONTAINER
Product Code
0264-7628
11-Digit Billing Format
00264762800
Billing Unit
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
RxNorm Crosswalk
  • RxCUI: 309783 - potassium chloride 20 MEQ / glucose 5 % in 1000 ML Injection
  • RxCUI: 309783 - 1000 ML glucose 50 MG/ML / potassium chloride 0.02 MEQ/ML Injection
  • RxCUI: 309783 - 1000 ML Glucose 50 MG/ML / K+ Chloride 0.02 MEQ/ML Injection
  • RxCUI: 309783 - 1000 ML Glucose 50 MG/ML / Pot Chloride 0.02 MEQ/ML Injection
  • RxCUI: 309783 - dextrose 5 % / potassium chloride 20 MEQ per 1000 ML Injection

Clinical Specifications

Proprietary Name
Potassium Chloride In Dextrose
Dosage Form
-
Usage Information
This intravenous solution is indicated for use in adults and pediatric patients as a source of electrolytes, calories, and water for hydration.

Regulatory & Marketing

Labeler Name
B. Braun Medical Inc.
FDA Application #
NDA019699
Marketing Category
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date
09-29-1989
End Marketing Date
03-31-2014
Listing Expiration
03-31-2014
Exclude Flag
D
Sample Package
No

Hierarchy Structure

Code Lineage

The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

* Please review the full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 0264-7628-00 identifies a specific commercial package of 12 container in 1 case / 1000 ml in 1 container of Potassium Chloride In Dextrose, labeled by B. Braun Medical Inc.. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by B. Braun Medical Inc. on September 29, 1989. The current certification is valid through March 31, 2014.

How is this B. Braun Medical Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 00264762800. Quantities are measured in per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (4-4-2)
0264-7628-00
11-Digit CMS (5-4-2)
00264-7628-00

Note: The zero is added to the Labeler segment to maintain the 5-4-2 structure.